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. 2024 Jan 19;35(2):e40. doi: 10.3802/jgo.2024.35.e40

Table 2. Tumor response in pMMR and all-comer populations.

Tumor response pMMR All-comer
Lenvatinib+pembrolizumab (n=66) TPC (n=68) Lenvatinib+pembrolizumab (n=77) TPC (n=78)
ORR*
% (95% CI) 36 (25–49) 22 (13–34) 39 (28–51) 21 (12–31)
BOR*
No. (%)
CR 6 (9.1) 3 (4.4) 9 (11.7) 4 (5.1)
PR 18 (27.3) 12 (17.6) 21 (27.3) 12 (15.4)
SD 25 (37.9) 25 (36.8) 28 (36.4) 30 (38.5)
PD 17 (25.8) 22 (32.4) 18 (23.4) 24 (30.8)
Not evaluable 0 (0.0) 1 (1.5) 0 (0.0) 1 (1.3)
No assessment 0 (0.0) 5 (7.4) 1 (1.3) 7 (9.0)
DOR (mo)
Median (range) 14.4 (1.6 to 39.5+) 5.2 (2.1+ to 37.1+) 16.5 (1.6 to 39.5+) 5.2 (1.9+ to 37.1+)

+, no PD by time of last assessment; BOR, best overall response; CR, complete response; DOR, duration of response; ORR, objective response rate; PD, progressive disease; pMMR, mismatch repair proficient; PR, partial response; SD, stable disease; TPC, treatment of physician’s choice chemotherapy.

*Per Response Evaluation Criteria in Solid Tumors version 1.1 by blinded independent central review.

Postbaseline assessment(s) available but not evaluable.

No postbaseline assessment available for response evaluation.